FDA applicant
Aus-Tex Dental Mfg. & Design
FDA records 3 decisions for Aus-Tex Dental Mfg. & Design (Mchenry, IL) from 1977 to 1981: 3 510(k) clearances. All are in product code EIC (Syringe, Periodontic, Endodontic, Irrigating). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Aus-Tex Dental Mfg. & Design’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Aus-Tex Dental Mfg. & Design since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Aus-Tex Dental Mfg. & Design’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report